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The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS
TrkA-mediated NGF signaling in PC12 cells has been shown to be compartimentalized in specialized microdomains of the plasma membrane, the caveolae, which are organized by scaffold proteins including the member of the caveolin family of proteins, caveolin-1. Here, we characterize the intracellular di...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765260/ https://www.ncbi.nlm.nih.gov/pubmed/24040018 http://dx.doi.org/10.1371/journal.pone.0073668 |
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author | Díaz-Ruiz, Alberto Rabanal-Ruiz, Yoana Trávez, Andrés Gracia-Navarro, Francisco Cruz-García, David Montero-Hadjadje, Maité Anouar, Youssef Gasman, Stéphane Vitale, Nicolas Vázquez-Martínez, Rafael Malagón, María M. |
author_facet | Díaz-Ruiz, Alberto Rabanal-Ruiz, Yoana Trávez, Andrés Gracia-Navarro, Francisco Cruz-García, David Montero-Hadjadje, Maité Anouar, Youssef Gasman, Stéphane Vitale, Nicolas Vázquez-Martínez, Rafael Malagón, María M. |
author_sort | Díaz-Ruiz, Alberto |
collection | PubMed |
description | TrkA-mediated NGF signaling in PC12 cells has been shown to be compartimentalized in specialized microdomains of the plasma membrane, the caveolae, which are organized by scaffold proteins including the member of the caveolin family of proteins, caveolin-1. Here, we characterize the intracellular distribution as well as the biochemical and functional properties of the neuroendocrine long coiled-coil protein 2 (NECC2), a novel long coiled-coil protein selectively expressed in neuroendocrine tissues that contains a predicted caveolin-binding domain and displays structural characteristics of a scaffolding factor. NECC2 distributes in caveolae, wherein it colocalizes with the TrkA receptor, and behaves as a caveolae-associated protein in neuroendocrine PC12 cells. In addition, stimulation of PC12 cells with nerve growth factor (NGF) increased the expression and regulated the distribution of NECC2. Interestingly, knockdown as well as overexpression of NECC2 resulted in a reduction of NGF-induced phosphorylation of the TrkA downstream effector extracellular signal-regulated kinases 1 and 2 (ERK1/ERK2) but not of Akt. Altogether, our results identify NECC2 as a novel component of caveolae in PC12 cells and support the contribution of this protein in the maintenance of TrkA-mediated NGF signaling. |
format | Online Article Text |
id | pubmed-3765260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37652602013-09-13 The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS Díaz-Ruiz, Alberto Rabanal-Ruiz, Yoana Trávez, Andrés Gracia-Navarro, Francisco Cruz-García, David Montero-Hadjadje, Maité Anouar, Youssef Gasman, Stéphane Vitale, Nicolas Vázquez-Martínez, Rafael Malagón, María M. PLoS One Research Article TrkA-mediated NGF signaling in PC12 cells has been shown to be compartimentalized in specialized microdomains of the plasma membrane, the caveolae, which are organized by scaffold proteins including the member of the caveolin family of proteins, caveolin-1. Here, we characterize the intracellular distribution as well as the biochemical and functional properties of the neuroendocrine long coiled-coil protein 2 (NECC2), a novel long coiled-coil protein selectively expressed in neuroendocrine tissues that contains a predicted caveolin-binding domain and displays structural characteristics of a scaffolding factor. NECC2 distributes in caveolae, wherein it colocalizes with the TrkA receptor, and behaves as a caveolae-associated protein in neuroendocrine PC12 cells. In addition, stimulation of PC12 cells with nerve growth factor (NGF) increased the expression and regulated the distribution of NECC2. Interestingly, knockdown as well as overexpression of NECC2 resulted in a reduction of NGF-induced phosphorylation of the TrkA downstream effector extracellular signal-regulated kinases 1 and 2 (ERK1/ERK2) but not of Akt. Altogether, our results identify NECC2 as a novel component of caveolae in PC12 cells and support the contribution of this protein in the maintenance of TrkA-mediated NGF signaling. Public Library of Science 2013-09-06 /pmc/articles/PMC3765260/ /pubmed/24040018 http://dx.doi.org/10.1371/journal.pone.0073668 Text en © 2013 Díaz-Ruiz et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Díaz-Ruiz, Alberto Rabanal-Ruiz, Yoana Trávez, Andrés Gracia-Navarro, Francisco Cruz-García, David Montero-Hadjadje, Maité Anouar, Youssef Gasman, Stéphane Vitale, Nicolas Vázquez-Martínez, Rafael Malagón, María M. The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title | The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title_full | The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title_fullStr | The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title_full_unstemmed | The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title_short | The Long Coiled-Coil Protein NECC2 Is Associated to Caveolae and MODULATES NGF/TrkA Signaling IN PC12 CELLS |
title_sort | long coiled-coil protein necc2 is associated to caveolae and modulates ngf/trka signaling in pc12 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765260/ https://www.ncbi.nlm.nih.gov/pubmed/24040018 http://dx.doi.org/10.1371/journal.pone.0073668 |
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